Regulatory Specialist

Heartflow; United States; On-site; USD 90,000 - 105,000; Full time

Job summary

An innovative medical technology company is seeking a Regulatory Specialist to join their Quality and Regulatory Affairs team. This entry-level position offers the opportunity to work with cutting-edge technology aimed at improving heart care. The role involves supporting regulatory activities, collaborating with cross-functional teams, and ensuring compliance with global regulations. If you are passionate about healthcare innovation and eager to contribute to a mission-driven organization, this is the perfect opportunity to make a meaningful impact in the medical field.

Qualifications

• 1-3 years of experience in Regulatory Affairs with compliance knowledge.
• Ability to resolve regulatory issues and maintain documentation.

Responsibilities

• Support software releases and EU MDR applications.
• Collaborate with teams for regulatory project management.
• Manage product registrations and maintain global approvals.

Skills

Global regulatory requirements

Project management

Team collaboration

Communication skills

Writing and editing skills

Word, Excel, PowerPoint

Education

Bachelor's degree

1-3 years in Regulatory Affairs

Software medical device experience

Job description

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Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product—an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFRCT Analysis—provides a color-coded, 3D model of a patient’s coronary arteries indicating the impact blockages have on blood flow to the heart. Heartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMapAnalysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). Our pipeline of products is growing and so is our team; join us in helping to revolutionize precision heartcare.

Heartflow is a VC-backed company that has received international recognition for exceptional strides in healthcare innovation, is supported by medical societies around the world, cleared for use in the US, UK, Europe, Japan and Canada, and has been used for more than 400,000 patients worldwide.

The Regulatory Affairs Specialist is part of the Quality and Regulatory Affairs team. The individual has 1-3 years of experience in Regulatory with an understanding of regulatory requirements and is able to resolve a wide-range of issues while maintaining compliance to regulations and standards. This individual will play a key role in HeartFlow regulatory activities involving cross-functional collaboration for product changes, as well as maintenance of key regulatory documentation. ;

Job Responsibilities:

• Support frequent minor software releases by performing change assessments
• Support EU MDR application and maintenance of technical documentation, including clinical evaluation
• Collaborate with cross-functional teams to drive regulatory project management activities
• Manage timely completion of new product registrations and maintain global regulatory approvals to market software devices
• Collaborate with external partners including regulatory agencies, authorized representatives, importers and distributors
• Gain experience with US FDA submissions
• Provide input to the risk management process to ensure risks are identified and updated during the product life-cycle
• Conduct regulatory surveillance and communicate changes in regulations., standards, and guidances
• Support Quality System management, as needed
• Other relevant duties as assigned
• Ability to work in a fast-paced adaptive environment, self-starter, and strong team player
  
  

Skills Needed:

• Base knowledge of global regulatory requirements
• Project management skills a plus
• Demonstrated team collaboration
• Excellent communication, writing, and editing skills
• Strong Word, Excel, and PowerPoint skills
  
  

Educational Requirements & Work Experience:

• Bachelor’s degree
• 1-3 years of experience in Regulatory Affairs
• Software medical device experience a plus
  
  

This position has an estimated base salary of $90,000 - $105,000, cash bonus, and stock options.

Heartflow is an Equal Opportunity Employer. We are committed to a work environment that supports, inspires, and respects all individuals and do not discriminate against any employee or applicant because of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. This policy applies to every aspect of employment at Heartflow, including recruitment, hiring, training, relocation, promotion, and termination.

Positions posted for Heartflow are not intended for or open to third party recruiters / agencies. Submission of any unsolicited resumes for these positions will be considered to be free referrals.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Legal

• Industries

  Medical Equipment Manufacturing

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